510(k) K802113 ยท DPS Electrocardiograph
SIRECUST 400 SYSTEM PATIENT MONITORING
| Applicant | Analogic Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 22, 1981 |
| Received | Sep 3, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802113
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.